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New balance system put to the test in teens with scoliosis

NCT ID NCT06224361

Knowledge-focused Sponsor: Istanbul University - Cerrahpasa Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study checks if a new balance assessment system gives consistent results in teenagers with scoliosis. Forty participants aged 12-18 with mild to moderate curves will perform balance tests twice, one week apart. The goal is to see if the tool is reliable for measuring postural stability, not to treat or improve the condition.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

40 people

The number who actually took part.

Started

Feb 2024

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adolescents diagnosed with adolescent idiopathic scoliosis between the ages of 12-18 who meet the inclusion criteria will be included in our study.

Ages

12 to 18 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Being between the ages of 12 and 18 * Having been diagnosed with Adolescent Idiopathic Scoliosis by an orthopedic specialist * Cobb angle measured on anteroposterior radiograph is below 40 degrees * Ability to understand and follow instructions * Volunteering to participate in the study Exclusion Criteria: * Presence of neuromuscular, rheumatic disease, or vestibular problems that may affect balance, vision-related diseases * Having a recent history of orthopedic injury or surgery in the lower extremity * Having had spine surgery * Not having experienced any acute situation that could affect postural stability and balance between the two tests (within 7 days) * Corset use has not changed between two tests (within 7 days)

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Conditions

The condition(s) this trial relates to.

adolescent idiopathic scoliosis scoliosis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Scoliosis; adolescence

Contacts and locations

Locations

  • Empatim Özel Eğitim ve Rehabilitasyon Merkezi

    Istanbul, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.